2-Benzyloxy-3-hexadecyloxypropyl 1,1-dimethylpyrrolidinio-2-ylmethyl phosphate → 3-Hexadecyloxy-2-hydroxypropyl 1,1-dimethylpyrrolidinio-2-ylmethyl phosphate

HRID 1088558Notes

Reaction equation

HRID 1088558 reaction equation
[P:1]([O-:41])([O:32][CH:33]=[C:34]1[CH2:38][CH2:37][CH2:36][N+:35]1([CH3:40])[CH3:39])([O:3][CH2:4][CH:5]([O:24]CC1C=CC=CC=1)[CH2:6][O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[O:2].[H][H]>C(O)C.[Pd]>[P:1]([O-:41])([O:32][CH:33]=[C:34]1[CH2:38][CH2:37][CH2:36][N+:35]1([CH3:40])[CH3:39])([O:3][CH2:4][CH:5]([OH:24])[CH2:6][O:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[O:2]

Participants

5

Procedure

In 20 ml of ethanol was dissolved 162 mg of 2-Benzyloxy-3-hexadecyloxypropyl 1,1-dimethylpyrrolidinio-2-ylmethyl phosphate prepared in Example 7, and 20 mg of palladium(5%)-carbon (catalyst) was added to the resulting solution. The mixture was stirred overnight at 50° C. in a stream of hydrogen. The reaction liquid was cooled, and the catalyst was removed by filtration. The filtrate was concentrated under reduced pressure to give 111 mg of 3-hexadecyloxy-2-hydroxypropyl 1,1-dimethylpyrrolidinio-2-ylmethyl phosphate.

Workup

  1. additionwas added to the resulting solution
  2. customThe reaction liquid
  3. temperaturewas cooled
  4. customthe catalyst was removed by filtration
  5. concentrationThe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-a14ef3f63dcc44cc8ebf411ff1bd4926
Source dataset
uspto-grants-1990_10
Patent number
US04962096

Reaction notes

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